Manufacturer registered with FDA
MK1 Dental-Attachment GmbH
Bockhorn, Germany. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 1
- 510(k) clearances
- 0as applicant
- Markets registered in
- 34 registrations outside the US
- Establishments
- 1Germany
Registered in 3 markets
Where regulators' registries name MK1 Dental-Attachment GmbH as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Manufacturer | MK1 Dental-Attachment GmbH | 1 device types | — | Below |
| European Union | EUDAMED | Manufacturer | MK1 Dental-Attachment GmbH | 3 | — | Pure Global AI |
| Brazil | ANVISA | Manufacturer | MK1 DENTAL ATTACHMENT GMBH | 1 | 2008–2008 | Pure Global AI |
Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026
Devices listed with FDA
What MK1 Dental-Attachment GmbH currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| All Precision AttachmentEGG · Class 1 | — | Maker | MK1 Dental-Attachment | 1991 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| MKI DENTAL PRODUKT GMBHFDA reg. 8043670 | Bockhorn Lower Saxony, Germany | Manufacturer |
Other names on FDA records
Mki Dental Produkt GmbH
Sources
FDA establishment registration & device listing (search FDA, owner/operator 9003136). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.